Medline Convenience Kits Recall Due to Adhesive Tubing Issue
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Medline Industries, LP is recalling 49,654 convenience kits nationwide because they contain a recalled lot of MASTISOL Liquid Adhesive with butyrate tubing that may crack.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 2, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Medline Industries, LP initiated a voluntary recall of certain convenience kits containing Ferndale Laboratories MASTISOL Liquid Adhesive. The butyrate tubing may crack during actuation and render the product unusable for application.
Which Products Are Affected
The recall covers 49,654 kits distributed nationwide in the United States. Affected products include:
- DAVINCI DYNJ905836D (Lot 25LBB534)
- DAVINCI-LF DYNJ905293I (Lot 25KBM585)
- GENERAL ROBOTICS PACK DYNJT8308 (Lot 26CBD040)
- GYN LAP CDS860087Q (Lots 25JBV094, 25LBP061)
- GYN LAPAROSCOPY DYNJ910084C (Lot 25LBE810)
- GYN LAPAROSCOPY CDS CDS982371I (Lots 25KBH343, 26CBN241)
- GYN LAPAROSCOPY CDS #34-RF CDS920099S (Lot 25KBO172)
- GYN LAPAROSCOPY PACK DYNJT3887 (Lot 25JBX564), DYNJT6876 (Lot 25KBM646)
- GYN ROBOTIC CDS CDS984228K (Lot 26ABF608)
- GYN ROBOTICS DYNJ911843 (Lot 25LBC203)
- KIT LABOR DELIVERY TUBAL LIGAT DYKMBNDL165C (Lot 25LBR024)
- ROBOTIC LAP CHOLE CDS CDS985442J (Lot 25JBT926)
- ROBOTIC PACK DYNJ84725B (Lot 25JBA329), DYNJ910594B (Lot 25KBJ104)
- ROBOTIC SURGERY PACK DYNJ53711B (Lots 25KBF929, 25LBB875)
- ROBOTICS PACK DYNJ83622C (Lots 25LBR740, 26CBJ460)
- UOFL GYN LAPAROSCOPY DYNJ909322B (Lot 25LBD961)
- WMC ROBOTIC PACK - LF DYNJ902583O (Lot 25LBC041)
Recall number Z-2431-2026. Classification: Class II.
What You Should Do
No specific consumer instructions are provided in the recall notice.
Why This Matters
This Class II recall affects kits used in surgical and procedural settings across the United States, with potential for product failure during use.
Source
FDA recall Z-2431-2026, report date 20260624.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,642 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 2, 2026.
Frequently Asked Questions
Common questions about this FDA recall.